UNC-39, the C-elegans homolog of the human myotonic dystrophy-associated homeodomain protein Six5, regulates cell motility and differentiation


Back to previous page
Authors: Yanowitz, JL; Shakir, MA; Hedgecock, E; Hutter, H; Fire, AZ; Lundquist, EA
Year: 2004
Journal: Developmental Biology 272: 389-402
Title: UNC-39, the C-elegans homolog of the human myotonic dystrophy-associated homeodomain protein Six5, regulates cell motility and differentiation
Abstract: Mutations in the unc-39 gene of C elegans lead to migration and differentiation defects in a subset of mesodermal and ectodermal cells, including muscles and neurons. Defects include mesodermal specification and differentiation as well a neuronal migration and axon pathfinding defects. Molecular analysis revealed that unc-39 corresponds to the previously named gene ceh-35 and that the UNC-39 protein belongs to the Six4/5 family of homeodomain transcription factors and is similar to human Six5, a protein implicated in the pathogenesis of type I myotonic dystrophy (DM1). We show that human Six5 and UNC-39 are functional homologs, suggesting that further characterization of the C. elegans unc-39 gene might provide insight into the etiology of DM1. (C) 2004 Elsevier Inc. All rights reserved.
Back to previous page
 

Please send suggestions for improving this publication database to sass-support@sfu.ca.
Departmental members may update their publication list.